Reaktion #74254

ord-ffac2490fbc3456483c73090f1c31fd7

Reaktionsgleichung

BrC1(Br)C2CCCCCC21
8,8-dibromobicyclo[5.1.0]octane
COC(=O)CO
methyl glycolate
[Al]
aluminum
COC(=O)C(O)C1CCCCCC=C1Br
17
Ausbeute 66.0%
COC(=O)C(O)C1CCCCCC=C1Br
methyl 2-bromocyclooct-1-en-3-glycolate
Ausbeute 66.0%

Lösungsmittel

Reaktionsbedingungen

Detaillierte Bedingungen
See reaction.notes.procedure_details.

Aufarbeitung

  1. 1
    Filtrationthe silver salts are filtered off through a sintered glass funnel
  2. 2
    Waschenwashed with AcOEt
  3. 3
    EinengenThe solution is concentrated under vacuum
  4. 4
    Sonstigeto give a viscous brown oil which
  5. 5
    Sonstigeis purified by chromatography on silica gel (cyclohexane/2-15% AcOEt)

Vorschrift

3.85 g of silver perchlorate (18.6 mmol) are added to a solution of 8,8-dibromobicyclo[5.1.0]octane 16 (2.5 g, 9.3 mmol) and methyl glycolate (6.35 ml, 83.9 mmol) dissolved in 5 ml of anhydrous toluene in a dry round-bottomed flask under Ar protected from light by an aluminum film. The reaction mixture is stirred at ambient temperature for 1 h 30 and then the silver salts are filtered off through a sintered glass funnel and washed with AcOEt. The solution is concentrated under vacuum to give a viscous brown oil which is purified by chromatography on silica gel (cyclohexane/2-15% AcOEt) to produce 17 in the form of a yellow oil (w=1.7 g, i.e. 66% yield).

Quelle

DOI: 10.6084/m9.figshare.5104873.v1Patent: US08541604B2uspto-grants-2013_09